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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >C-type natriuretic peptide modulates glutamate receptors on cultured rat retinal amacrine cells.
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C-type natriuretic peptide modulates glutamate receptors on cultured rat retinal amacrine cells.

机译:C型利钠肽可调节培养的大鼠视网膜无长突细胞上的谷氨酸受体。

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摘要

C-type natriuretic peptide, widely distributed in the CNS, may work as a neuromodulator. In this work, we investigated modulation by C-type natriuretic peptide of functional properties of glutamate receptors in rat retinal GABAergic amacrine cells in culture. Immunocytochemical data revealed that natriuretic peptide receptor-B was strongly expressed on the membrane of cultured GABAergic amacrine cells. By whole cell recording techniques we further identified the glutamate receptor expressed on the GABAergic amacrine cells as an AMPA-preferring subtype. Incubation with C-type natriuretic peptide suppressed the AMPA receptor-mediated current of these cells in a dose-dependent manner by decreasing the efficacy and apparent affinity for glutamate. The effect of C-type natriuretic peptide was reversed by HS-142-1, a guanylyl cyclase-coupled natriuretic peptide receptor-A/B antagonist. Meanwhile, the selective natriuretic peptide receptor-C agonist cANF did not change the glutamate current. In conjunction with the immunocytochemical data, these results suggest that the C-type natriuretic peptide effect may be mediated by natriuretic peptide receptor-B. Furthermore, incubation of retinal cultures in the C-type natriuretic peptide-containing medium elevated cGMP immunoreactivity in the GABAergic amacrine cells, and the C-type natriuretic peptide effect on the glutamate current was mimicked by application of 8-Br-cGMP. It is therefore concluded that C-type natriuretic peptide may modulate the glutamate current by increasing the intracellular concentration of cGMP in these cells via activation of natriuretic peptide receptor-B.
机译:广泛分布在中枢神经系统中的C型利钠肽可能起神经调节剂的作用。在这项工作中,我们研究了通过C型利钠肽对培养的大鼠视网膜GABA能amacrine细胞中谷氨酸受体功能特性的调节。免疫细胞化学数据显示,利尿钠肽受体B在培养的GABA能的无长突细胞膜上强烈表达。通过全细胞记录技术,我们进一步鉴定了在GABA能的无长突细胞上表达的谷氨酸受体为AMPA优先亚型。与C型利尿钠肽一起孵育可降低剂量和对谷氨酸的表观亲和力,从而以剂量依赖的方式抑制AMPA受体介导的这些细胞的电流。胍基环化酶偶联的利钠肽受体-A / B拮抗剂HS-142-1逆转了C型利钠肽的作用。同时,选择性利钠肽受体-C激动剂cANF不会改变谷氨酸电流。结合免疫细胞化学数据,这些结果表明,C型利钠肽的作用可能是由利钠肽受体B介导的。此外,在含有C型利钠肽的培养基中培养视网膜培养物可提高GABA能的无长突细胞中cGMP的免疫反应性,并通过应用8-Br-cGMP来模拟C型利尿肽对谷氨酸电流的作用。因此得出结论,C型利钠肽可以通过利钠肽受体-B的激活来增加这些细胞中cGMP的细胞内浓度,从而调节谷氨酸电流。

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